We went to Utah for a week this summer. We were able to go see Stadium of Fire at BYU. The Jonas Brothers (or as Lauren calls them..The JoBros's) were in concert. We had really good seats in the stadium , but I still snuck her down on the field, almost up to the front row so she could get a better look. She had a blast. Josh's favorite part was the military flyover at the very beginning. He thought that was awesome.
We also went to Lagoon. Hope was able to ride a lot of the little kiddies rides with her brother or her cousins. She loved it.
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We also went to a new water park in Draper called KowaBunga Bay. It was another very fun day.
When I got back from Utah, I was feeling very run down. I talked to my Oncologist about it, and she moved my September CAT scan up to July. She said the cancer is stable, my lymph nodes have not grown any, so that was good to hear. She did think I might want to consider a round of Rituxin therapy. It is an immunotherapy, and is not as harsh on your system as chemotherapy. She said it would shrink all my lymph nodes down, and could help with some of the symptoms I've been having. The down side is, it would be a 2 year treatment. It is a 4 hour IV drip once a week for a month. And then 2 months off. I'm just not sure I'm ready to commit to that yet. The last month I've actually felt great. So I'm going to wait until my follow up appt in September to discuss that option. Not sure I'm mentally ready for any treatment. I'm liking this "watch & wait" because it allows to me to live a normal life. But I'm not opposed to the treatment if I start to feel like the symptoms are getting worse. I still take it one day at a time! And so far...the days have been pretty darn great!
When I got back from Utah, I was feeling very run down. I talked to my Oncologist about it, and she moved my September CAT scan up to July. She said the cancer is stable, my lymph nodes have not grown any, so that was good to hear. She did think I might want to consider a round of Rituxin therapy. It is an immunotherapy, and is not as harsh on your system as chemotherapy. She said it would shrink all my lymph nodes down, and could help with some of the symptoms I've been having. The down side is, it would be a 2 year treatment. It is a 4 hour IV drip once a week for a month. And then 2 months off. I'm just not sure I'm ready to commit to that yet. The last month I've actually felt great. So I'm going to wait until my follow up appt in September to discuss that option. Not sure I'm mentally ready for any treatment. I'm liking this "watch & wait" because it allows to me to live a normal life. But I'm not opposed to the treatment if I start to feel like the symptoms are getting worse. I still take it one day at a time! And so far...the days have been pretty darn great!
1 comment:
Miss Jen, I've missed your posts...glad you're back! :0) What a great summer full of family!! You are such a great example of staying positive no matter what comes your way! Did you ever know that you're my hero?!
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